Different mechanisms underlie three inhibitory phenomena in cat area 17

Vision Research

Volumn 38, Issue 14, 1998, Pages 2067-2080

  Sengpiel, Frank ^a   Baddeley, Roland J ^a   Freeman, Tobe C B ^a   Harrad, Richard ^a   Blakemore, Colin ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Contrast; Gain control; Inhibition; Primary visual cortex; Suppression

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; CAT; CONTRAST; CONTRAST SENSITIVITY; CONTROLLED STUDY; EYE DOMINANCE; GRATING; INHIBITORY POSTSYNAPTIC POTENTIAL; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; VISUAL CORTEX; VISUAL FIELD; VISUAL STIMULATION;

ACTION POTENTIALS; ANIMALS; BRAIN MAPPING; CATS; NEURAL INHIBITION; PATTERN RECOGNITION, VISUAL; ROTATION; VISUAL CORTEX;

EID: 0031869078     PISSN: 00426989     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0042-6989(97)00413-6     Document Type: Article

References (64)

1. Hubel D.H. Receptive fields of single neurones in the cat's striate cortex. Journal of Physiology. 148:1959;574-591.
2. Hubel D.H., Wiesel T.N. Receptive fields, binocular interaction and functional architecture in the cat's visual cortex. Journal of Physiology. 160:1962;106-154.
3. Creutzfeldt O.D., Kuhnt U., Benevento L.A. An intracellular analysis of visual cortical neurones to moving stimuli: responses in a co-operative neuronal network. Experimental Brain Research. 21:1974;251-274.
4. Blakemore C., Tobin E.A. Lateral inhibition between orientation detectors in the cat's visual cortex. Experimental Brain Research. 15:1972;439-440.
5. Bishop P.O., Coombs J.S., Henry G.H. Receptive fields of simple cells in the cat striate cortex. Journal of Physiology. 231:1973;31-60.
6. Rose D., Blakemore C. Effects of bicuculline on functions of inhibition in visual cortex. Nature. 249:1974;375-377.
7. Sillito A.M. The contribution of inhibitory mechanisms to the receptive field properties of neurones in the striate cortex of the cat. Journal of Physiology. 250:1975;305-329.
8. Sillito A.M. Inhibitory mechanisms influencing complex cell orientation selectivity and their modification at high resting discharge levels. Journal of Physiology. 289:1979;33-53.
9. Eysel U.T., Crook J.M., Machemer H.F. GABA-induced remote inactivation reveals cross-orientation inhibition in the cat striate cortex. Experimental Brain Research. 80:1990;626-630.
10. Crook J.M., Eysel U.T. GABA-induced inactivation of functionally characterised sites in cat visual cortex (area 18): effects on orientation tuning. Journal of Neuroscience. 12:1992;1816-1825.
11. DeAngelis G.C., Robson J.G., Ohzawa I., Freeman R.D. Organization of suppression in receptive fields of neurons in cat striate cortex. Journal of Neurophysiology. 68:1992;144-163.
12. Morrone M.C., Burr D.C., Maffei L. Functional implications of cross-orientation inhibition of cortical visual cells. I. Neurophysiological evidence. Proceedings of the Royal Society (London) Series B. 216:1982;335-354.
13. Morrone M.C., Burr D.C., Speed H.D. Cross-orientation inhibition in cat is GABA mediated. Experimental Brain Research. 67:1987;635-644.
14. Hubel D.H., Wiesel T.N. Receptive fields and functional architecture in two non-striate visual areas (18 and 19) of the cat. Journal of Neurophysiology. 28:1965;229-289.
15. Orban G.A., Kato H., Bishop P.O. Dimensions and properties of end-zone inhibitory areas in receptive fields of hypercomplex cells in cat striate cortex. Journal of Neurophysiology. 42:1979;833-849.
16. Nelson J.I., Frost B.J. Orientation-selective inhibition from beyond the classic visual receptive field. Brain Research. 139:1978;359-365.
17. Sillito A.M., Versiani V. The contribution of excitatory and inhibitory inputs to the length preference of hypercomplex cells in layers II and III of the cat's striate cortex. Journal of Physiology. 273:1977;775-790.
18. Bolz J., Gilbert C.D., Wiesel T.N. Pharmacological analysis of cortical circuitry. Trends in Neurosciences. 12:1989;292-296.
19. Grieve K.L., Sillito A.M. A re-appraisal of the role of layer VI of the visual cortex in the generation of cortical end inhibition. Experimental Brain Research. 87:1991;521-529.
20. Murphy P.C., Sillito A.M. Corticofugal feedback influences the generation of length tuning in the visual pathway. Nature. 329:1987;727-729.
21. Sengpiel F., Blakemore C. Interocular control of neuronal responsiveness in cat visual cortex. Nature. 368:1994;847-850.
22. Sengpiel F., Blakemore C., Harrad R. Interocular suppression in the primary visual cortex: a possible neural basis of binocular rivalry. Vision Research. 35:1995;179-195.
23. Sengpiel F., Freeman T.C.B., Blakemore C. Interocular suppression in cat striate cortex is not orientation selective. NeuroReport. 6:1995;2235-2239.
24. Ullman S., Schechtman G. Adaptation and gain normalisation. Proceedings of the Royal Society (London) Series B. 216:1982;299-313.
25. Heeger D.J. Normalization of cell responses in cat striate cortex. Visual Neuroscience. 9:1992;181-197.
26. Bonds A.B. Role of inhibition in the specification of orientation selectivity of cells in the cat striate cortex. Visual Neuroscience. 2:1989;41-55.
27. DeAngelis G.C., Freeman R.D., Ohzawa I. Length and width tuning of neurons in the cat's primary visual cortex. Journal of Neurophysiology. 71:1994;347-374.
28. Sengpiel F., Sen A., Blakemore C. Characteristics of surround inhibition in cat area 17. Experimental Brain Research. 116:1997;216-228.
29. Ohzawa I., Sclar G., Freeman R.D. Contrast gain control in the cat visual cortex. Nature. 298:1982;266-268.
30. Ohzawa I., Sclar G., Freeman R.D. Contrast gain control in the cat's visual system. Journal of Neurophysiology. 54:1985;651-667.
31. DeBruyn E.J., Bonds A.B. Contrast adaptation in cat visual cortex is not mediated by GABA. Brain Research. 383:1986;339-342.
32. McLean J., Palmer L.A. Contrast adaptation and excitatory amino acid receptors in cat striate cortex. Visual Neuroscience. 13:1996;1069-1087.
33. Sengpiel F., Blakemore C., Kind P.C., Harrad R. Interocular suppression in the visual cortex of strabismic cats. Journal of Neuroscience. 14:1994;6855-6871.
34. Sengpiel F., Baddeley R.J., Freeman T.C.B., Harrad R., Blakemore C. Two different mechanisms underlie suppressive phenomena in cat primary visual cortex. Society for Neuroscience Abstracts. 21:1995;1649.
35. Freeman T.C.B., Sengpiel F., Blakemore C. Interocular suppression and binocular facilitation in cat primary visual cortex as a function of stimulus contrast. Brain Research Association Abstracts. 13:1996;78.
36. Skottun B.C., DeValois R.L., Grosof D.H., Movshon J.A., Albrecht D.G., Bonds A.B. Classifying simple and complex cells on the basis of response modulation. Vision Research. 31:1991;1079-1086.
37. Barlow H.B., Blakemore C., Pettigrew J.D. The neural mechanism of binocular depth perception. Journal of Physiology. 193:1967;327-342.
38. Albrecht D.G., Hamilton D.B. Striate cortex of monkey and cat: contrast response function. Journal of Neurophysiology. 48:1982;217-237.
39. Albrecht D.G. Visual cortex neurons in monkey and cat: effect of contrast on the spatial and temporal phase transfer functions. Visual Neuroscience. 12:1995;1191-1210.
40. Tolhurst D.J., Heeger D.J. Comparison of contrast-normalisation and threshold models of the responses of simple cells in cat striate cortex. Visual Neuroscience. 14:1997;293-309.
41. Nelder J.A., Mead R. A simplex method for function minimization. Computer Journal. 7:1965;308-313.
42. Press W.H., Flannery B.P., Teukolsky S.A., Vetterling W.T. Numerical Recipes in C. 1992;Cambridge University Press, Cambridge.
43. Bonds A.B. Temporal dynamics of contrast gain in single cells of the cat striate cortex. Visual Neuroscience. 6:1991;239-255.
44. Bonds A.B. The encoding of cortical contrast gain control. Shapley R., Lam D.M.-K. Contrast Sensitivity. 1993;215-230 MIT Press, Cambridge, MA.
45. Albus K., Wahle P. The topography of tangential inhibitory connections in the postnatally developing and mature striate cortex of the cat. European Journal of Neuroscience. 6:1994;779-792.
46. Kisvárday Z.F., Kim D.-S., Eysel U.T., Bonhoeffer T. Relationship between lateral inhibitory connections and the topography of the orientation map in cat visual cortex. European Journal of Neuroscience. 6:1994;1619-1632.
47. Tong L., Guido W., Tumosa N., Spear P.D., Heidenreich S. Binocular interactions in the cat's dorsal lateral geniculate nucleus, II: Effects on dominant-eye spatial frequency and contrast processing. Visual Neuroscience. 8:1992;557-566.
48. Ahmed B., Anderson J.C., Douglas R.J., Martin K.A.C., Nelson J.C. Polyneuronal innervation of spiny stellate neurons in cat visual cortex. Journal of Comparative Neurology. 341:1994;39-49.
49. Ahmed B., Anderson J.C., Martin K.A.C., Nelson J.C. Map of the synapses onto layer 4 basket cells of the primary visual cortex of the cat. Journal of Comparative Neurology. 380:1997;230-242.
50. Allison J.D., Dinger J., Bonds A.B., Casagrande V.A. The contribution of LGN M and P layers to the contrast sensitivity of primate V1 neurons. Society for Neuroscience Abstracts. 21:1995;1648.
51. Fox R., Check R. Independence between binocular rivalry suppression duration and magnitude of suppression. Journal of Experimental Psychology. 93:1972;283-289.
52. Blake R., Fox R. Binocular rivalry suppression: insensitive to spatial frequency and orientation change. Vision Research. 14:1974;687-692.
53. Holopigian K. Clinical suppression and binocular rivalry suppression: the effects of stimulus strength on the depth of suppression. Vision Research. 29:1989;1325-1333.
54. Campbell F.W., Kulikowski J.J. Orientational selectivity of the human visual system. Journal of Physiology. 187:1966;437-445.
55. Snowden R.J., Hammett S.T. Subtractive and divisive adaptation in the human visual system. Nature. 355:1992;248-250.
56. Georgeson M.A. The effect of spatial adaptation on perceived contrast. Spatial Vision. 1:1985;103-112.
57. Knierim J.J., Van Essen D.C. Neuronal responses to static texture patterns in area V1 of the alert macaque monkey. Journal of Neurophysiology. 67:1992;961-980.
58. Toth L.J., Rao S.C., Kim D.-S., Somers D., Sur M. Subthreshold facilitation and suppression in primary visual cortex revealed by intrinsic signal imaging. Proceedings of the National Academy of Sciences USA. 93:1996;9869-9874.
59. Levitt J.B., Lund J.S. Contrast dependence of contextual effects in primate visual cortex. Nature. 387:1997;73-76.
60. Cannon M.W., Fullenkamp S.C. Spatial interactions in apparent contrast: individual differences in enhancement and suppression effects. Vision Research. 33:1993;1685-1695.
61. Polat U., Sagi D. Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments. Vision Research. 33:1993;993-999.
62. Polat U., Norcia A.M. Neurophysiological evidence for contrast dependent long-range facilitation and suppression in the human visual cortex. Vision Research. 36:1996;2099-2109.
63. Stemmler M., Usher M., Niebur E. Lateral interactions in primary visual cortex: a model bridging physiology and psychophysics. Science. 269:1995;1877-1880.
64. Somers D.C., Todorov E.V., Siapas A.G., Toth L.J., Kim D.-S., Sur M. 1998 A local circuit approach to understanding integration of long-range inputs in primary visual cortex. Cerebral Cortex, in press.